Package 0615-8605-39
Brand: amantadine
Generic: amantadinePackage Facts
Identity
Package NDC
0615-8605-39
Digits Only
0615860539
Product NDC
0615-8605
Description
30 TABLET in 1 BLISTER PACK (0615-8605-39)
Marketing
Marketing Status
Brand
amantadine
Generic
amantadine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a8ae3043-8fe8-4e56-9829-a53b597c4910", "openfda": {"unii": ["M6Q1EO9TD0"], "rxcui": ["849395"], "spl_set_id": ["2ff05131-f634-4688-86e9-9bc33a8d11c4"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (0615-8605-39)", "package_ndc": "0615-8605-39", "marketing_start_date": "20260120"}], "brand_name": "Amantadine", "product_id": "0615-8605_a8ae3043-8fe8-4e56-9829-a53b597c4910", "dosage_form": "TABLET", "pharm_class": ["Influenza A M2 Protein Inhibitor [EPC]", "M2 Protein Inhibitors [MoA]"], "product_ndc": "0615-8605", "generic_name": "Amantadine", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amantadine", "active_ingredients": [{"name": "AMANTADINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA214284", "marketing_category": "ANDA", "marketing_start_date": "20201020", "listing_expiration_date": "20271231"}